CLOZAPINE

Product NDC: 57664-241
11-digit product format: 576640241
Labeler code: 57664
Product ID: 57664-241_5dab493f-f2b8-4841-9332-1d9d97451460
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: CLOZAPINE
Dosage form: TABLET
Route: ORAL
Labeler: Sun Pharmaceutical Industries, Inc.
Application: ANDA075713
Marketing category: ANDA
Marketing start: 2005-08-19
Marketing end: 0000-00-00
Substance: CLOZAPINE
Active strength: 50 mg/1
Pharmacologic classes: Atypical Antipsychotic [EPC]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fde12e54-43fa-cc16-3015-4c000a7b8d3e	Product name	5	20250812
0901063f-b37f-4bf1-8be6-1e2a469e57bc	Product name	2	20180209
e01fb60f-a608-2c68-dfdd-23e6433ece68	Product name	5	20180209
7a7f58c4-be43-7e82-4dfc-128bbed4230a	Product name	1	20140508

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
429212	cloZAPine 50 MG Oral Tablet	PSN	9b035a6a-f5c1-43a8-9203-cc016dc6e422	106
429212	clozapine 50 MG Oral Tablet	SCD	9b035a6a-f5c1-43a8-9203-cc016dc6e422	106

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
57664-241-13	57664024113	500 TABLET in 1 BOTTLE (57664-241-13)	500 tablet	2005-08-19	0000-00-00	No	No	Current
57664-241-88	57664024188	100 TABLET in 1 BOTTLE (57664-241-88)	100 tablet	2005-08-19	0000-00-00	No	No	Current